Hey, you left out Henoch-Schoenlein Purpura, the type of renal failure that killed Mozart! It is not a statistically important cause of renal failure, but I had to mention it because I just love to say, "Henoch-Schoenlein."
Hey, you left out Henoch-Schoenlein Purpura, the type of renal failure that killed Mozart! It is not a statistically important cause of renal failure, but I had to mention it because I just love to say, "Henoch-Schoenlein."
Gee, and all this time I thought it was called, "Hammacher Schlemmer Syndrome."
;)
Hey, you left out Henoch-Schoenlein Purpura, the type of renal failure that killed Mozart! It is not a statistically important cause of renal failure, but I had to mention it because I just love to say, "Henoch-Schoenlein."
Gee, and all this time I thought it was called, "Hammacher Schlemmer Syndrome."
;)
A catalog service? ???
So I have my interview with the transplant surgeon and he tells me my kidney failure was not caused by high blood pressure and all my other tests come back negative as far as the cause goes. :-\
Can we change our vote? I had chosen type 1 diabetes, but since then, my doctors have decided it was due to hospital error.Hospital Error? :o ::) :urcrazy;
Can we change our vote? I had chosen type 1 diabetes, but since then, my doctors have decided it was due to hospital error.
Not sure exactly. I was admitted to Johns Hopkins Hospital back in 2005 for a bronchitis like cough and vomiting up blood. They told me it was asthma (WTF?!). I was uninsured, so the next day they kicked me out. In the 24 hours I was there, I swelled up with fluid, putting on 30 pounds of water weight, and got an infection going up my entire arm from the IV. And they still kicked me out. Right after that, my kidneys statred to fail. Thinking back, I should have sued the hospital, but I had no proof by that point. I ended up with a $13,000 hospital bill and ended up declaring bankruptcy as a result. :banghead; :banghead; :banghead;Sorry to hear,
As for me, it is only believed to be Alports Syndrome as my Uncle had it too along with deafness as do I. We're not sure though as the tissue in my biopsy was too far gone for them to be sure. The symptoms however, all support Alports and what is interesting is that I was initially given anti - inflammotary pain killers for foot pain which may or may not have killed off any remaining kidney function I had left.
Do you have health insurance (besides Medicare)? That should cover hearing aids.
Mine was caused by dysplastic horseshoe kidney which is both rare and hereditary. Whenever I am having an utrasound for something else, everyone asks if they can take a look at my horseshoe as they haven't see one before. Nothing unusual there. It just looks like a horseshoe with two kidney beans at each end.
Mine was glomerulonephritis of unknown origin! By the time I was diagnosed I was already end stage and my Nephrologist said there wasn't any way of knowing for sure. My doctors and surgeons now days say it was probably a Staph infection.
Hey, you left out Henoch-Schoenlein Purpura, the type of renal failure that killed Mozart! It is not a statistically important cause of renal failure, but I had to mention it because I just love to say, "Henoch-Schoenlein." "Schoenlein" is also German for "pretty little thing," a term of endearment sometimes used among lovers there, but it does not describe the horrors of that disease very well!
I got it from primary hyperparathyroidism. Which I guess is really uncommon. I had it, undiagnosed, for about 10 years -- there were quite a few opportunities for it to be caught before it took my kidneys out, but hey, my medical clinic mislaid my bloodwork for 5 years. :rofl;
Yeh, most renal patients suffer from secondary Hyper pth- it happens as a result of the renal failure and had it not been for the renal failure we never would have gotten it.
I hope I didn't leave anything out, please let me know. Feel free to explain.
I cant find it, but my friend had strep throat that lead to his kidney failure.
Lisa
This has been a very intereresting thread, to me, to read. Thanks to all for sharing. I had not idea there were so many possible causes.
My loss was due to injury. I noticed that I was the first respondent with that cause.
For those who like details, here goes. I was working, a deputy sheriff, saw a fellow I knew to be wanted coming out of the back door of a closed business at three in the morning. He fled, I persued. He ran his car through a corn field and come out and ran into mine. Another deputy close by caught him. I am on dialysis and his is in prison. No winners.
When I was in my early 30th my doctor told me I had high blood pressure. However, I felt I was too young to have hbp so I totally ignored him. WHY DID I DO THAT? Young and foolish, I decided to continue going on with life without trying to lower my BP.I had the blurred vision and found out i had high bp (215/125) the same day i started dialysis. Although it took weeks for my sight to recover.
So one day I woke up and everything around me was blurry. I could not see anything. I went to the doctor and they could not tell me what was wrong although the doctor office took so many tests. I must have saw about 10 different doctors and not one of them decided to take my BP. To make a long story short, I winded up in the hospital after I could not breath and fell out. The doctors in the hospital decided to take my BP and found out it was 200/120. Right there and than the doctor gave me some meds. I started to get my sight back after several hours. That's when the doctor told me I had to go on dailysis. I was so upset. I've tried every herbs I could afford. It worked but I couldn't paid $150 a week to maintain the herbs. So after 6 months and behind on my rent. I decided to go on dailysis. It was so hard for me. I cried for about one year hoping my kidneys will start functioning again. After a year I became very angry whereas I pushed everyone out of my life. Well, they stayed away for a while. After three years on dailysis, I started to fell sorry for myself. Then after five years felling sorry for myself and not really interacting with to many people, I was thinking about killing myself. It was time for me to see a psychologist, which changed my whole attitude.... I started to accept dailysis and reunited with my friends and family and started to live again. Now I'm more positive and have a great career and dating. POSITIVE THOUGHTS, POSITIVE ENERGY!
When I was in my early 30th my doctor told me I had high blood pressure. However, I felt I was too young to have hbp so I totally ignored him. WHY DID I DO THAT?
So one day I woke up and everything around me was blurry. I could not see anything. I went to the doctor and they could not tell me what was wrong although the doctor office took so many tests.
The doctors in the hospital decided to take my BP and found out it was 200/120.
So after 6 months and behind on my rent. I decided to go on dailysis. It was so hard for me. I cried for about one year hoping my kidneys will start functioning again. After a year I became very angry whereas I pushed everyone out of my life. Well, they stayed away for a while. After three years on dailysis, I started to fell sorry for myself. Then after five years felling sorry for myself and not really interacting with to many people, I was thinking about killing myself. It was time for me to see a psychologist, which changed my whole attitude.... I started to accept dailysis and reunited with my friends and family and started to live again. Now I'm more positive and have a great career and dating. POSITIVE THOUGHTS, POSITIVE ENERGY!
Hmm its seems like i am in the 'majority' here ! I wonder if they just lump us all together because they cant give us any explanation or reason as to why its happened ? Focal Glomerulosclerosis is looking mighty popular ! I wonder should we take this poll a step futher and ask what reasons they gave you when this was diagnosed ? I myself have never been given a reason for kidney failure .. one day fit and healthy , get up next morning .. i got kidney failure !! yup that fast .. no outward signs or illness , all overnight it happened !!
I voted hypertension but I think it complicated it. Come to think of it they didn't ever tell me why my kidneys failed, thats probably a question I need to ask...or maybe they did tell me and I wasn't listening as usual. Just ask my wife, I hear really good but I do not listen.
The reason I lost my kidneys were due to Cyctinosis. Cystinosis is a lysosomal storage disease characterized by the abnormal accumulation of the amino acid cystine in the cells.
I don't know why I have fsgs, either. The prevailing theory is that my pregancy in 1991 was the catalyst. My son feels bad because he thinks he caused it. :'(
I don't know why I have fsgs, either. The prevailing theory is that my pregancy in 1991 was the catalyst. My son feels bad because he thinks he caused it. :'(
Strange, because had i not had my son, i wouldnt know i had kidney failure.
Hello
I don't know if I am doing this right but I am new to this site and I am trying to figure out how I post my opinions and views about my hating dialysis. Can someone help me please!
Other. My mother after giving birth to my sister 1996 began having protein in her urine. Her doctors never raised a concern about this until the spring of 2012. I 2012 her primary doctor told her that she needs to see a neurologist, through out the 2 months she was going to this doctor he put her on meds that made her gain a lot of weight (steroids) then told us she needed to have a biopsy done. Summer 2012 we had biopsy done, doctor told us it was an infection to continue taking meds, didn't tell us if this was life threading or anything. 6 months later this doctor resigns( what the???) my mom was feeling fine so we didn't even really think to find a new doctor .. But I said she needed to go so I scheduled an appt summer 13. Went to the new neph. And when I showed him the biopsy report he said OMG! Her kidney function was 15% at this point. He scheduled a new biopsy and later explained to us, that my moms own body was attacking the kidney. He never gave us a name but said she would need to start dialysis really soon. In the months leading to sept. Everything declined , my mom went from 15% kidney function to 2% over 2 days. Now she's on dialysis, she is still peeing. I don't really know what to call what she has, dies anyone know??This sounds like an auto immune disease, which means the body's immune system is attacking the persons own body . Many times the kidneys are the target. It may be IgA nephropathy which is one type and there are others it also could be. That is probably why she was put on prednisone(steroids) as it reduces the immune system actions. Many people still urinate while on dialysis but the kidneys arent functioning correctly or enough.